A novel homozygous mutation of the EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2007.08206.x/fullpdf
Reference11 articles.
1. Evidence for a Nonallelic Heterogeneity of Epidermodysplasia Verruciformis with Two Susceptibility Loci Mapped to Chromosome Regions 2p21–p24 and 17q25
2. Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis
3. Detection of human papillomavirus (HPV) type 47 DNA in malignant lesions from epidermodysplasia verruciformis by protocols for precise typing of related HPV DNAs
4. X-linked inheritance of epidermodysplasia verruciformis. Genetic and virologic studies of a kindred
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1. Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review;Genetics in Medicine;2024-02
2. Aggressive Squamous Cell Carcinoma in a Case of Epidermodysplasia Verruciformis Carrying a TMC6 Splice-site Mutation;Acta Dermato-Venereologica;2023-01-27
3. Cervical dysplasia in a patient with inherited epidermodysplasia verruciformis—A mere coincidence?;Journal of Cutaneous Pathology;2020-12-22
4. Gene expression is stable in a complete CIB1 knockout keratinocyte model;Scientific Reports;2020-09-11
5. EVER1 and EVER2 Mutations in Epidermodysplasia Verruciformis;Encyclopedia of Medical Immunology;2020
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